So far, we have put the loaded spheres in PBS and measured concentration via ELISA at different time points (one sample per time point). Any idea if spectrophotometry could be used for this? If so, how? Thanks!
Dear Justin Markel
Pls. find the attached files
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0127174
http://pubs.acs.org/doi/abs/10.1021/nn3057005
https://www.ebioscience.com/media/pdf/best-protocols/cytokine-neutralization-in-vitro.pdf
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1821039/
http://www.ebioscience.com/resources/best-protocols/functional-activity-protocols.htm
http://www.bdbiosciences.com/anz/resources/protocols/cytokine_elisa.jsp
http://www.sciencedirect.com/science/article/pii/S1567576911002256
http://media.ebioscience.com/data/pdf/best-protocols/cytokine-neutralization-in-vitro.pdf
http://media.ebioscience.com/data/pdf/best-protocols/cytokine-bioassays.pdf
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0058208
http://www.nature.com/articles/srep15400
http://www.omicsonline.org/open-access/evaluation-of-invitro-antiinflammatory-activity-of-silver-nanoparticlessynthesised-using-piper-nigrum-extract-2157-7439-1000268.php?aid=41236
Regards
Prof. Houda Kawas
Why thank you, Professor. I will look into this.
You most welcome
Houda
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